Hepatitis C virus infection in 2012 and beyond

W. Abuelhassan
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引用次数: 8

Abstract

Hepatitis C virus infection is estimated to affect 150 million people worldwide. A large number of individuals are chronically infected and are at risk of developing chronic liver disease, cirrhosis and hepatocellular carcinoma. Chronic hepatitis C infection causes significant morbidity and mortality. It is the leading indication for liver transplantation in the USA and Europe, and accounts for 30-50% of liver transplants in those countries. The introduction of blood and blood product screening protocols in 1992 led to a decline in new infections, but intravenous drug abuse still remains a major risk factor for acquiring the disease. Since no vaccine is available to prevent infection with this virus, research has been ongoing to find a cure. Treatment of hepatitis C has continuously evolved since the introduction of interferon monotherapy in the early 1990s, with very low response rates. In 2002, the use of pegylated interferon and ribavirin significantly improved sustained virological response rates to 50-80%. The management of patients who do not respond to standard care remains challenging. The US FDA approved directly acting antivirals in May 2011. This introduced a new era with regard to management of this condition.
2012年及以后丙型肝炎病毒感染情况
估计全世界有1.5亿人感染丙型肝炎病毒。许多人受到慢性感染,并有发展为慢性肝病、肝硬化和肝细胞癌的危险。慢性丙型肝炎感染导致显著的发病率和死亡率。它是美国和欧洲肝移植的主要适应症,占这些国家肝移植的30-50%。1992年开始实行血液和血液制品检查规程,导致新感染人数下降,但静脉注射药物滥用仍然是感染该病的一个主要危险因素。由于没有疫苗可以预防这种病毒的感染,因此一直在进行寻找治疗方法的研究。自20世纪90年代初引入干扰素单药治疗以来,丙型肝炎的治疗方法不断发展,但反应率非常低。2002年,聚乙二醇化干扰素和利巴韦林的使用显著提高了持续病毒学应答率至50-80%。对标准治疗无效的患者的管理仍然具有挑战性。美国食品和药物管理局于2011年5月批准了直接作用的抗病毒药物。这为这种疾病的管理开创了一个新时代。
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